Does DRONEDARONE Cause Wrong technique in product usage process? 50 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 50 reports of Wrong technique in product usage process have been filed in association with DRONEDARONE (Multaq). This represents 1.8% of all adverse event reports for DRONEDARONE.
50
Reports of Wrong technique in product usage process with DRONEDARONE
1.8%
of all DRONEDARONE reports
0
Deaths
7
Hospitalizations
How Dangerous Is Wrong technique in product usage process From DRONEDARONE?
Of the 50 reports, 7 (14.0%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DRONEDARONE. However, 50 reports have been filed with the FAERS database.
What Other Side Effects Does DRONEDARONE Cause?
Atrial fibrillation (309)
Dyspnoea (235)
Fatigue (206)
Off label use (189)
Drug interaction (176)
Nausea (151)
Diarrhoea (141)
Dizziness (136)
Drug ineffective (128)
Asthenia (101)
What Other Drugs Cause Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which DRONEDARONE Alternatives Have Lower Wrong technique in product usage process Risk?
DRONEDARONE vs DROPERIDOL
DRONEDARONE vs DROSPIRENONE
DRONEDARONE vs DROSPIRENONE\ESTETROL
DRONEDARONE vs DROSPIRENONE\ESTRADIOL
DRONEDARONE vs DROSPIRENONE\ETHINYL ESTRADIOL